CCSER2[gene] and "single gene"[properties] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 57

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2244572	NM_001284240.2(CCSER2):c.26C>G (p.Thr9Arg)	CCSER2 (T9R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140155	NM_001284240.2(CCSER2):c.65C>T (p.Ser22Phe)	CCSER2 (S22F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3264664	NM_001284240.2(CCSER2):c.127A>G (p.Lys43Glu)	CCSER2 (K43E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140144	NM_001284240.2(CCSER2):c.143A>G (p.Lys48Arg)	CCSER2 (K48R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455637	NM_001284240.2(CCSER2):c.151A>G (p.Ile51Val)	CCSER2 (I51V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2259673	NM_001284240.2(CCSER2):c.245C>T (p.Pro82Leu)	CCSER2 (P82L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140151	NM_001284240.2(CCSER2):c.374C>G (p.Ala125Gly)	CCSER2 (A125G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140152	NM_001284240.2(CCSER2):c.379C>T (p.Pro127Ser)	CCSER2 (P127S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2250175	NM_001284240.2(CCSER2):c.385A>G (p.Thr129Ala)	CCSER2 (T129A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216088	NM_001284240.2(CCSER2):c.500A>G (p.Asn167Ser)	CCSER2 (N167S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3140153	NM_001284240.2(CCSER2):c.568G>A (p.Ala190Thr)	CCSER2 (A190T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3264667	NM_001284240.2(CCSER2):c.610G>A (p.Ala204Thr)	CCSER2 (A204T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140154	NM_001284240.2(CCSER2):c.620C>A (p.Pro207Gln)	CCSER2 (P207Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3264665	NM_001284240.2(CCSER2):c.679T>A (p.Ser227Thr)	CCSER2 (S227T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209332	NM_001284240.2(CCSER2):c.703C>G (p.Pro235Ala)	CCSER2 (P235A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2237191	NM_001284240.2(CCSER2):c.710C>G (p.Ser237Cys)	CCSER2 (S237C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518082	NM_001284240.2(CCSER2):c.716C>T (p.Thr239Ile)	CCSER2 (T239I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241797	NM_001284240.2(CCSER2):c.773A>G (p.Gln258Arg)	CCSER2 (Q258R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2614452	NM_001284240.2(CCSER2):c.841A>G (p.Asn281Asp)	CCSER2 (N281D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140156	NM_001284240.2(CCSER2):c.842A>G (p.Asn281Ser)	CCSER2 (N281S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140157	NM_001284240.2(CCSER2):c.934A>G (p.Thr312Ala)	CCSER2 (T312A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220644	NM_001284240.2(CCSER2):c.946A>G (p.Arg316Gly)	CCSER2 (R316G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384769	NM_001284240.2(CCSER2):c.1000A>G (p.Met334Val)	CCSER2 (M334V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2240004	NM_001284240.2(CCSER2):c.1016A>C (p.Asn339Thr)	CCSER2 (N339T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207637	NM_001284240.2(CCSER2):c.1274A>G (p.Asn425Ser)	CCSER2 (N425S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2336463	NM_001284240.2(CCSER2):c.1298A>G (p.Glu433Gly)	CCSER2 (E433G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140143	NM_001284240.2(CCSER2):c.1316A>C (p.Glu439Ala)	CCSER2 (E439A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398305	NM_001284240.2(CCSER2):c.1321C>T (p.His441Tyr)	CCSER2 (H441Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461559	NM_001284240.2(CCSER2):c.1340A>G (p.Gln447Arg)	CCSER2 (Q447R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207311	NM_001284240.2(CCSER2):c.1406T>C (p.Ile469Thr)	CCSER2 (I469T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272350	NM_001284240.2(CCSER2):c.1589A>G (p.Tyr530Cys)	CCSER2 (Y530C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2326255	NM_001284240.2(CCSER2):c.1677T>A (p.Asp559Glu)	CCSER2 (D559E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140146	NM_001284240.2(CCSER2):c.1681C>T (p.Pro561Ser)	CCSER2 (P561S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380004	NM_001284240.2(CCSER2):c.1726C>T (p.Arg576Cys)	CCSER2 (R576C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2212886	NM_001284240.2(CCSER2):c.1727G>A (p.Arg576His)	CCSER2 (R576H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140147	NM_001284240.2(CCSER2):c.1736G>A (p.Arg579Gln)	CCSER2 (R579Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140148	NM_001284240.2(CCSER2):c.1753C>T (p.Arg585Trp)	CCSER2 (R12W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542410	NM_001284240.2(CCSER2):c.1768G>A (p.Gly590Ser)	CCSER2 (G590S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484308	NM_001284240.2(CCSER2):c.1777A>G (p.Lys593Glu)	CCSER2 (K20E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140149	NM_001284240.2(CCSER2):c.1810C>A (p.His604Asn)	CCSER2 (H604N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458325	NM_001284240.2(CCSER2):c.1838A>G (p.Tyr613Cys)	CCSER2 (Y40C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404385	NM_001284240.2(CCSER2):c.1891C>A (p.Pro631Thr)	CCSER2 (P58T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140150	NM_001284240.2(CCSER2):c.1928T>C (p.Phe643Ser)	CCSER2 (F643S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216468	NM_001284240.2(CCSER2):c.2033A>G (p.Gln678Arg)	CCSER2 (Q105R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610338	NM_001284240.2(CCSER2):c.2172A>G (p.Ile724Met)	CCSER2 (I151M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3264663	NM_001284240.2(CCSER2):c.2188G>A (p.Glu730Lys)	CCSER2 (E157K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3264666	NM_001284240.2(CCSER2):c.2246A>T (p.His749Leu)	CCSER2 (H176L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241601	NM_001284240.2(CCSER2):c.2326-13558C>T	CCSER2 (P781L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2621281	NM_001284240.2(CCSER2):c.2326-13552T>C	CCSER2 (F210S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2394815	NM_001284240.2(CCSER2):c.2326-13543G>T	CCSER2 (W786L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3264661	NM_001284240.2(CCSER2):c.2326-13535T>G	CCSER2 (S216A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2616466	NM_001284240.2(CCSER2):c.2326-13498G>A	CCSER2 (R801H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2477749	NM_001284240.2(CCSER2):c.2341C>T (p.Pro781Ser)	CCSER2 (P208S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3264662	NM_001284240.2(CCSER2):c.2395C>T (p.Pro799Ser)	CCSER2 (A254V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2509324	NM_001284240.2(CCSER2):c.2400A>G (p.Gln800=)	CCSER2 (T256A +1 more)	Single nucleotide variant (synonymous variant +2 more)	not specified	GLikely benign
Select item 2394629	NM_001284240.2(CCSER2):c.2407G>A (p.Glu803Lys)	CCSER2 (R258Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 563757	GRCh37/hg19 10q23.1(chr10:86086359-86817361)x1	CCSER2	Copy number loss	not provided	GUncertain significance

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 57